Document Detail


alpha-Sarcoglycan (adhalin) deficiency: complete deficiency patients are 5% of childhood-onset dystrophin-normal muscular dystrophy and most partial deficiency patients do not have gene mutations.
MedLine Citation:
PMID:  8866424     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
alpha-Sarcoglycan (adhalin), a 50-kDa component of the dystrophin-associated complex of proteins, participates in the stabilization of the myofiber plasma membrane in the membrane cytoskeleton. Deficiencies of alpha-sarcoglycan cause a subset of childhood-onset muscular dystrophy (SCARMD) cases. However, secondary deficiencies of alpha-sarcoglycan are common. To begin to establish the rates of false positives (secondary deficiencies), we used immunofluorescence to screen 30 Italian dystrophin-normal muscular dystrophy patient biopsies and identified 4 patients with partial alpha-sarcoglycan deficiency and 2 patients with complete deficiency. The entire alpha-sarcoglycan gene was screened for mutations using RT-PCR and SSCP of messenger RNA isolated from muscle biopsies in each of the six patients. Aberrant SSCP conformers and novel mutations were found only in the two complete immunohistochemical deficient patients. One patient was homozygous for a R34H amino acid substitution, while the other was a compound heterozygote (R77C, D97G). These three missense mutations, with additional mutations we and others have previously described, are all localized in the extracellular domain of alpha-sarcoglycan, and most result in the loss or gain of a positively charged amino acid. These data have strong implications for structure/function maps of the alpha-sarcoglycan molecule. Our results suggest that most patients showing partial alpha-sarcoglycan deficiency exhibit this as a secondary consequence of genetically distinct disorders. In support of this, we show biochemical data indicating that secondary deficiency patients show decreased immunostaining with antibodies directed against alpha-sarcoglycan, while having nearly normal quantities of alpha-sarcoglycan protein on immunoblot. This data also suggests that approximately 5% of childhood-onset dystrophin-normal muscular dystrophy patients will show a primary alpha-sarcoglycan deficiency.
Authors:
D J Duggan; M Fanin; E Pegoraro; C Angelini; E P Hoffman
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Publication Detail:
Type:  Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Journal of the neurological sciences     Volume:  140     ISSN:  0022-510X     ISO Abbreviation:  J. Neurol. Sci.     Publication Date:  1996 Sep 
Date Detail:
Created Date:  1997-01-03     Completed Date:  1997-01-03     Revised Date:  2012-05-09    
Medline Journal Info:
Nlm Unique ID:  0375403     Medline TA:  J Neurol Sci     Country:  NETHERLANDS    
Other Details:
Languages:  eng     Pagination:  30-9     Citation Subset:  IM    
Affiliation:
Department of Human Genetics, University of Pittsburgh School of Medicine, University of Pittsburgh, PA 15261, USA.
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MeSH Terms
Descriptor/Qualifier:
Base Sequence
Cytoskeletal Proteins / analysis,  deficiency*
Dystrophin / genetics*
Humans
Immunoblotting
Membrane Glycoproteins / analysis,  deficiency*
Molecular Sequence Data
Muscular Dystrophies / genetics*,  metabolism*
Mutation*
RNA, Messenger / metabolism
Sarcoglycans
Grant Support
ID/Acronym/Agency:
695//Telethon; C.19//Telethon
Chemical
Reg. No./Substance:
0/Cytoskeletal Proteins; 0/Dystrophin; 0/Membrane Glycoproteins; 0/RNA, Messenger; 0/Sarcoglycans

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